Taiwan FDA registration 416cdc4a5e175abc641180f75d9ceb3b

"Yikang" powered treatment unit (unsterilized)

TW: "一康" 動力式治療檯 (未滅菌)

Taiwan·Risk Class 1·GUANGZHOU YIKANG MEDICAL EQUIPMENT INDUSTRIAL CO., LTD·Registered Sep 22, 2015 – Sep 22, 2020Cancelled

Registration details

Analysis ID: 416cdc4a5e175abc641180f75d9ceb3b
Customs Code: DHA09600250200

Company information

Manufacturer: GUANGZHOU YIKANG MEDICAL EQUIPMENT INDUSTRIAL CO., LTD
Manufacturer Country: China
Authorized Representative: CONTINUOUS INSTRUMENT CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Powered Treatment Units (O.3760)".
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.3760 Powered therapy cage
Import Information: Chinese goods;; input

Dates and status

Registration Date: Sep 22, 2015
Expiry Date: Sep 22, 2020
Cancellation Date: May 19, 2022

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for "Yikang" powered treatment unit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 416cdc4a5e175abc641180f75d9ceb3b and manufactured by GUANGZHOU YIKANG MEDICAL EQUIPMENT INDUSTRIAL CO., LTD. The authorized representative in Taiwan is CONTINUOUS INSTRUMENT CO., LTD..

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